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原纤维形成胶原蛋白I、II和III在人骨关节炎软骨细胞中的独立表达。

Independent expression of fibril-forming collagens I, II, and III in chondrocytes of human osteoarthritic cartilage.

作者信息

Aigner T, Bertling W, Stöss H, Weseloh G, von der Mark K

机构信息

Department of Pathology, University of Erlangen-Nürnberg, Germany.

出版信息

J Clin Invest. 1993 Mar;91(3):829-37. doi: 10.1172/JCI116303.

DOI:10.1172/JCI116303
PMID:7680669
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC288034/
Abstract

Normal and osteoarthritic human articular cartilage was investigated by in situ hybridization for expression patterns of the fibrillar collagens type I, II, and III to evaluate phenotypic changes of articular chondrocytes related to the disease. In 11 out of 20 samples, a defined subset of chondrocytes in the superficial and upper middle zone of osteoarthritic cartilage showed significant levels of cytoplasmic alpha 1 (III) mRNA, whereas strong signals of alpha 1 (II) mRNA were found in the upper and lower middle zone, partially overlapping with the zone of alpha 1 (III) mRNA-expressing cells. The extent of type II and III collagen expression depended on the integrity of the extracellular matrix surrounding the chondrocytes, and the location within the articular cartilage. No alpha 1 (I) mRNA was detectable in osteoarthritic original articular cartilage. The alpha 1 (I) probe did, however, reveal signals in pannus-like tissue, osteophytes, and bone cells. In normal articular cartilage, no detectable levels of cytoplasmic mRNA for alpha 1(I), alpha 2 (I), or alpha 1 (III) were seen. Using specific mono- and polyclonal antibodies, we found deposition of type III collagen but hardly any of type I collagen in the superficial zone of osteoarthritic cartilage that is consistent with the in situ hybridization results. These results indicate a phenotypic alteration in a defined subset of chondrocytes in conditions of diseased cartilage, expressing and synthesizing collagen type III independently from type I collagen, but in part simultaneously with type II collagen.

摘要

通过原位杂交研究正常和骨关节炎患者的关节软骨中I型、II型和III型纤维胶原的表达模式,以评估与该疾病相关的关节软骨细胞的表型变化。在20个样本中的11个样本中,骨关节炎软骨表层和中上区的特定软骨细胞亚群显示出显著水平的细胞质α1(III)mRNA,而α1(II)mRNA的强信号则出现在中上层和中下层,部分与表达α1(III)mRNA的细胞区域重叠。II型和III型胶原的表达程度取决于软骨细胞周围细胞外基质的完整性以及在关节软骨中的位置。在骨关节炎原始关节软骨中未检测到α1(I)mRNA。然而,α1(I)探针在血管翳样组织、骨赘和骨细胞中显示出信号。在正常关节软骨中,未检测到α1(I)、α2(I)或α1(III)的细胞质mRNA水平。使用特异性单克隆和多克隆抗体,我们发现骨关节炎软骨表层存在III型胶原沉积,但几乎没有I型胶原沉积,这与原位杂交结果一致。这些结果表明,在患病软骨条件下,特定软骨细胞亚群发生了表型改变,独立于I型胶原表达和合成III型胶原,但部分与II型胶原同时表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c02f/288034/366931705c37/jcinvest00038-0103-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c02f/288034/3fbd7a5d48ee/jcinvest00038-0100-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c02f/288034/504745d6ddea/jcinvest00038-0101-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c02f/288034/fda3606c98e5/jcinvest00038-0102-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c02f/288034/366931705c37/jcinvest00038-0103-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c02f/288034/3fbd7a5d48ee/jcinvest00038-0100-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c02f/288034/504745d6ddea/jcinvest00038-0101-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c02f/288034/fda3606c98e5/jcinvest00038-0102-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c02f/288034/366931705c37/jcinvest00038-0103-a.jpg

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